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Diabetic nephropathy, also known as diabetic kidney disease, [5] is the chronic loss of kidney function occurring in those with diabetes mellitus. Diabetic nephropathy is the leading causes of chronic kidney disease (CKD) and end-stage renal disease (ESRD) globally. The triad of protein leaking into the urine (proteinuria or albuminuria ...
Complications of Wilson's disease can include liver failure and kidney problems. A liver transplant may be helpful to those for whom other treatments are not effective or if liver failure occurs. [1] Wilson's disease occurs in about one in 30,000 people. [1] Symptoms usually begin between the ages of 5 and 35 years. [1]
Angiopathy is the generic term for a disease of the blood vessels (arteries, veins, and capillaries). [1] This also refers to the condition of damage or rupture of small blood vessels. The best known and most prevalent angiopathy is diabetic angiopathy , a common complication of chronic diabetes .
An eponymous disease is a disease, disorder, condition, or syndrome named after a person, usually the physician or other health care professional who first identified the disease; less commonly, a patient who had the disease; rarely, a literary character who exhibited signs of the disease or an actor or subject of an allusion, as characteristics associated with them were suggestive of symptoms ...
Wilson's (temperature) syndrome, also called Wilson's thyroid syndrome or WTS, is a term used in alternative medicine to improperly attribute various common and non-specific symptoms to abnormally low body temperature and impaired conversion of thyroxine (T4) to triiodothyronine (T3), despite normal thyroid function tests. [1] E.
Kimmelstiel and Wilson introduced the term diabetic nephropathy (DN) to define a clinical syndrome of arterial hypertension, overt proteinuria (or macroalbuminuria), and worsening kidney function (Kimmelstiel and Wilson, 1936a). [4] Wilson returned to the London Hospital. He graduated DM in 1936. [3]
Wilson disease protein (WND), also known as ATP7B protein, is a copper-transporting P-type ATPase which is encoded by the ATP7B gene. The ATP7B protein is located in the trans-Golgi network of the liver and brain and balances the copper level in the body by excreting excess copper into bile and plasma.
Kimmelstiel-Wilson syndrome; Kindler syndrome; King–Kopetzky syndrome; Kleine–Levin syndrome; Klinefelter syndrome; Klippel–Feil syndrome; Klippel–Trénaunay syndrome; Klüver–Bucy syndrome; Knobloch syndrome; Kocher–Debre–Semelaigne syndrome; Kohlschütter-Tönz syndrome; Korsakoff's syndrome; Kostmann syndrome; Kounis syndrome ...